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RAZEK EQUIPAMENTOS LTDA

US

Last updated May 23, 2026

What RAZEK EQUIPAMENTOS LTDA makes

The company produces single-use orthopaedic burs designed for surgical procedures, as well as reusable orthopaedic surgical procedure kits that do not contain medications. These tools are intended for use in orthopaedic surgeries where precision cutting or preparation of bone is required.

The portfolio consists of Class I devices, which are generally considered to pose the lowest risk and are subject to minimal regulatory oversight. These devices are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. regulatory requirements. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Razek Equipamentos Ltda manufacture?

Razek Equipamentos Ltda produces two primary types of orthopaedic devices: single-use orthopaedic burs, which are designed for precise cutting or bone preparation during surgery, and reusable orthopaedic surgical procedure kits that do not contain medications. These tools are specifically intended for orthopaedic procedures where controlled bone manipulation is required.

Where is Razek Equipamentos Ltda based?

Razek Equipamentos Ltda is based in the United States. The company’s location influences its regulatory compliance, particularly in relation to U.S. requirements for device classification and traceability.

How are Razek Equipamentos Ltda’s devices classified under U.S. regulations?

Razek Equipamentos Ltda’s devices fall under Class I classification, which is the lowest risk category for medical devices in the U.S. This classification applies to products like single-use burs and reusable orthopaedic kits that pose minimal risk to patients. Class I devices typically require less regulatory scrutiny, though they must still meet basic safety and performance standards.

Are Razek Equipamentos Ltda’s devices listed in any regulatory databases?

Yes, Razek Equipamentos Ltda’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system ensures traceability and compliance by assigning a unique identifier to each device, helping track its distribution, usage, and regulatory status. This is particularly important for Class I devices, which must still adhere to labeling and manufacturing requirements.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
—
LinkedIn
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Facebook
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Email
—
Phone
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PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 190 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 733390300
FDA UDI
Class IActive
Razek Equipamentos 738350190
FDA UDI
Class IActive
Razek Equipamentos 732791400
FDA UDI
Class IActive
Razek Equipamentos 730010003
FDA UDI
Class IActive
Razek Equipamentos 974240000
FDA UDI
Class IActive
Razek Equipamentos 736880200
FDA UDI
Class IActive
Razek Equipamentos 978880360
FDA UDI
Class IActive
Razek Equipamentos 738740340
FDA UDI
Class IActive
Razek Equipamentos 738741230
FDA UDI
Class IActive
Razek Equipamentos 738701130
FDA UDI
Class IActive
Razek Equipamentos 978360800
FDA UDI
Class IActive
Razek Equipamentos 738180270
FDA UDI
Class IActive
Razek Equipamentos 738870410
FDA UDI
Class IActive
Razek Equipamentos 490061510
FDA UDI
Class IActive
Razek Equipamentos 736470500
FDA UDI
Class IActive
Razek Equipamentos 736221000
FDA UDI
Class IActive
Razek Equipamentos 738640060
FDA UDI
Class IActive
Razek Equipamentos 735530100
FDA UDI
Class IActive
Razek Equipamentos 730510007
FDA UDI
Class IActive
Razek Equipamentos 732850400
FDA UDI
Class IActive
Razek Equipamentos 978851130
FDA UDI
Class IActive
Razek Equipamentos 732761300
FDA UDI
Class IActive
Razek Equipamentos 973450000
FDA UDI
Class IActive
Razek Equipamentos 972750000
FDA UDI
Class IActive
Razek Equipamentos 978827500
FDA UDI
Class IActive
Razek Equipamentos 738880080
FDA UDI
Class IActive
Razek Equipamentos 738110460
FDA UDI
Class IActive
Razek Equipamentos 736101200
FDA UDI
Class IActive
Razek Equipamentos 978640700
FDA UDI
Class IActive
Razek Equipamentos 736430400
FDA UDI
Class IActive
Razek Equipamentos 978740500
FDA UDI
Class IActive
Razek Equipamentos 736320900
FDA UDI
Class IActive
Razek Equipamentos 730430000
FDA UDI
Class IActive
Razek Equipamentos 736030300
FDA UDI
Class IActive
Razek Equipamentos 732810100
FDA UDI
Class IActive
Razek Equipamentos 731560000
FDA UDI
Class IActive
Razek Equipamentos 730140000
FDA UDI
Class IActive
Razek Equipamentos 978850150
FDA UDI
Class IActive
Razek Equipamentos 978851490
FDA UDI
Class IActive
Razek Equipamentos 738941060
FDA UDI
Class IActive
Razek Equipamentos 738080080
FDA UDI
Class IActive
Razek Equipamentos 736610400
FDA UDI
Class IActive
Razek Equipamentos 738130230
FDA UDI
Class IActive
Razek Equipamentos 730240009
FDA UDI
Class IActive
Razek Equipamentos 974530000
FDA UDI
Class IActive
Razek Equipamentos 978780100
FDA UDI
Class IActive
Razek Equipamentos 979010070
FDA UDI
Class IActive
Razek Equipamentos 738370200
FDA UDI
Class IActive
Razek Equipamentos 978960030
FDA UDI
Class IActive
Razek Equipamentos 978861550
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Razek Equipamentos Ltda Sao Carlos Sao Paulo · BR FEI 3021907852